Medical Device Recalls
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1 result found
510(K) Number: K983003 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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MassTRANSIT Infusion Catheter Kit, 605-731K & 605-780K, Cordis Neurovascular Intended to be used ... | 2 | 12/30/2008 | Cordis Corporation |
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